Retinoic acid induces human gastruloids with posterior embryo-like structures

Nat Cell Biol. 2024 Oct;26(10):1790-1803. doi: 10.1038/s41556-024-01487-8. Epub 2024 Aug 20.

Abstract

Gastruloids are a powerful in vitro model of early human development. However, although elongated and composed of all three germ layers, human gastruloids do not morphologically resemble post-implantation human embryos. Here we show that an early pulse of retinoic acid (RA), together with later Matrigel, robustly induces human gastruloids with posterior embryo-like morphological structures, including a neural tube flanked by segmented somites and diverse cell types, including neural crest, neural progenitors, renal progenitors and myocytes. Through in silico staging based on single-cell RNA sequencing, we find that human RA-gastruloids progress further than other human or mouse embryo models, aligning to E9.5 mouse and CS11 cynomolgus monkey embryos. We leverage chemical and genetic perturbations of RA-gastruloids to confirm that WNT and BMP signalling regulate somite formation and neural tube length in the human context, while transcription factors TBX6 and PAX3 underpin presomitic mesoderm and neural crest, respectively. Looking forward, RA-gastruloids are a robust, scalable model for decoding early human embryogenesis.

MeSH terms

  • Animals
  • Embryo, Mammalian / drug effects
  • Embryo, Mammalian / metabolism
  • Embryonic Development / drug effects
  • Gastrula / drug effects
  • Gastrula / metabolism
  • Gene Expression Regulation, Developmental / drug effects
  • Humans
  • Macaca fascicularis / embryology
  • Mesoderm / drug effects
  • Mesoderm / embryology
  • Mesoderm / metabolism
  • Mice
  • Neural Crest* / drug effects
  • Neural Crest* / embryology
  • Neural Crest* / metabolism
  • Neural Tube / drug effects
  • Neural Tube / embryology
  • Neural Tube / metabolism
  • PAX3 Transcription Factor* / genetics
  • PAX3 Transcription Factor* / metabolism
  • Signal Transduction / drug effects
  • Somites* / drug effects
  • Somites* / embryology
  • Somites* / metabolism
  • T-Box Domain Proteins* / genetics
  • T-Box Domain Proteins* / metabolism
  • Tretinoin* / metabolism
  • Tretinoin* / pharmacology
  • Wnt Signaling Pathway / drug effects

Substances

  • Tretinoin
  • T-Box Domain Proteins
  • PAX3 Transcription Factor
  • PAX3 protein, human